14797-55-8Relevant articles and documents
Chemical and Electrochemical Oxidation of Solutions of Silver Nitrate in Acetonitrile
Tracy, Mark L.,Nash, Charles P.
, p. 1239 - 1242 (1985)
In anhydrous acetonitrile the unstable, brown species Ag(NO3)42-, I, can be produced either by the electrolysis of silver nitrate or by the equilibrium reaction N2O5 + Ag+ + 3NO3- ->/-3.The ESR spectrum of I at 77 K is that of a Ag(II) ion in a field with pronounced axial distortion.Its resonance Raman spectrum indicates square-planar coordination of the metal ion by unidentate nitrate ligands.The complex decomposes to form cyanomethyl nitrate and nitric acid by the rate law -d/dt = k/->.In the presence of p-xylene a major organic product is p-methylbenzyl nitrate.Equilibrium and electrochemical studies lead to estimated ΔG0298 values for the free radical and ionic dissociation pathways of N2O5 in acetonitrile solution of +38 and -26 kJ, respectively.
Nucleophile Assistance of Electron-Transfer Reactions between Nitrogen Dioxide and Chlorine Dioxide Concurrent with the Nitrogen Dioxide Disproportionation
Becker, Robert H.,Nicoson, Jeffrey S.,Margerum, Dale W.
, p. 7938 - 7944 (2003)
The reaction of chlorine dioxide with excess NO2- to form ClO2- and NO3- in the presence of a large concentration of ClO2- is followed via stopped-flow spectroscopy. Concentrations are set to establish a preequilibrium among ClO2, NO2-, ClO2-, and an intermediate, NO2. Studies are conducted at pH 12.0 to avoid complications due to the ClO2-/NO2- reaction. These conditions enable the kinetic study of the ClO2 reaction with nitrogen dioxide as well as the NO2 disproportionation reaction. The rate of the NO2/ClO2 electron-transfer reaction is accelerated by different nucleophiles (NO2- > Br- > OH- > CO32- > PO43- > ClO2- > H 2O). The third-order rate constants for the nucleophile-assisted reactions between NO2 and ClO2 (kNu, M -2 s-1) at 25.0 °C vary from 4.4 × 10 6 for NO2- to 2.0 × 103 when H2O is the nucleophile. The nucleophile is found to associate with NO2 and not with ClO2 in the rate-determining step to give NuNO2+ + ClO2-. The concurrent NO2 disproportionation reaction exhibits no nucleophilic effect and has a rate constant of 4.8 × 107 M-1 s -1. The ClO2/NO2/nucleophile reaction is another example of a system that exhibits general nucleophilic acceleration of electron transfer. This system also represents an alternative way to study the rate of NO2 disproportionation.
HYPOCHLORITE OXIDATION OF AMMONIA. EFFECTIVE REMOVAL OF AMMONIA FROM WASTE WATER BY UV-IRRADIATION.
Kimura,Suzuki,Ogata
, p. 3198 - 3201 (1980)
The hypochlorite oxidation of ammonia giving rise to nitrogen evolution was carried out in the dark or under irradiation in order to study the reaction mechanism and application to waste water treatment. UV-irradiation accelerates remarkably the rate of decomposition of unfavorable chloramines. The acceleration covers the pH region 2-12, where corresponding dark reactions are slow. The irradiation also affects the formation of byproducts such as NO//2** minus and NO//3** minus , the effect being a slight increase in NO//2** minus formation in the pH range 2-12. These results suggest an effective industrial application to avoid eutrophication in seas and lakes. The irradiation effect is discussed in relation to reaction mechanism, in which the irradiation possibly facilitates the N-N bond formation after chloramine formation.
NMR study of reactions between Pd, Ru, and Rh nitrite complexes with sulfamic acid
Belyaev,Emel'yanov,Khranenko,Fedotov
, p. 184 - 194 (2001)
Reactions of nitrite complexes of Pd, Ru, and Rh with sulfamic acid were studied by the 14, 15N, and 17O NMR method. Chemical shifts were assigned, and the predominant forms of the complexes were established. The reaction products at room temperature are cis-nitroaqua complexes. Coordination of the sulfamate ion upon storage for a long time or on heating was detected.
Nanopore enriched hollow carbon nitride nanospheres with extremely high visible-light photocatalytic activity in the degradation of aqueous contaminants of emerging concern
Yang, Yuxin,Hu, An,Wang, Xinyue,Meng, Jiaqi,Guo, Yihang,Huo, Mingxin,Zhu, Suiyi
, p. 355 - 365 (2019/01/28)
Construction of highly efficient hollow nanosphere photocatalytic systems has been strongly attracting the attention of researchers. In the present work, nanopore enriched hollow carbon nitride nanospheres (HCNNSs) with a smaller particle size (200 nm) and a thinner shell thickness (40 nm) are successfully fabricated by a silica-nanocasting strategy. Such unique structures possess many advantages such as large BET surface area (122 m2 g-1), high light-harvesting ability, fast charge separation and transfer efficiency, plentiful exposed active sites and enhanced oxidation ability of photogenerated holes (h+VB). Therefore, HCNNSs in smaller sizes (HCNNS-200) exhibit extremely excellent visible-light photocatalytic efficiency towards the degradation of contaminants of emerging concern, e.g. levofloxacin (LEVO), in comparison with bulk g-C3N4 and HCNNSs in larger sizes (HCNNS-500). And it takes less than 10 min to finish the degradation of LEVO. The experimental results including those from indirect chemical probing, electron spin resonance, ion chromatography and high performance liquid chromatography-mass spectrometry confirm that h+VB and O2- are the active species that are responsible for the mineralization of LEVO to NO3-, F-, H2O and CO2 under visible-light irradiation. Additionally, the degradation pathway of LEVO in the HCNNS-200 photocatalytic system is also proposed. It is expected that HCNNS-200 can be used as a promising photocatalyst for environmental remediation.
Design and construction of a bifunctional magnetically recyclable 3D CoMn2O4/CF hybrid as an adsorptive photocatalyst for the effective removal of contaminants
Zheng, Jianhua,Hu, Yandong,Zhang, Lei
, p. 25044 - 25051 (2017/09/29)
Herein, a magnetic microsphere CoMn2O4 (MS-CoMn2O4) with a 3D architecture was constructed directly on cellulose fiber (CF) substrates from wastepaper by a solvothermal synthesis method with further calcination treatment. The designed hybrid shows excellent dual functions including rapid catalytic oxidation of tetracycline (TC)/methylene blue (MB) and a high adsorption capacity. What's more, the hybrid is easily recycled using an external magnetic field. In comparison with that of pure MS-CoMn2O4, the enhanced adsorption ability and photocatalytic activity of MS-CoMn2O4/CFs can mainly be attributed to the introduced cellulose fiber supporter in the hybrid system. MS-CoMn2O4 incorporated CFs can improve the efficient separation of photogenerated electron-hole pairs and the transport pathway of electrons. More importantly, introduction of CFs can help to enrich and further improve the degradation efficiency of organic contaminants. The possible mechanism for the enhancement of the photocatalytic activity has been elucidated in detail. The reusability analysis revealed that the MS-CoMn2O4/CF hybrid exhibited superb cycling stability after 5 cycles. This study provides novel insights into the design and construction of high capacity sorbents as strongly adsorptive photocatalysts to perform catalytic degradation of organic contaminants.